ATG16L1 Primary Antibody

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Description
The protein encoded by this gene is part of a large protein complex that is necessary for autophagy, the major process by which intracellular components are targeted to lysosomes for degradation. Defects in this gene are a cause of susceptibility to inflammatory bowel disease type 10 (IBD10). Several transcript variants encoding different isoforms have been found for this gene.
Product Overview
Formulation
Purified antibody in PBS with 0.05% sodium azide
Storage
4°C; -20°C for long term storage
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Elisa
Figure 1: Black line: Control Antigen (100 ng); Purple line: Antigen(10ng); Blue line: Antigen (50 ng); Red line: Antigen (100 ng);
Figure 1: Black line: Control Antigen (100 ng); Purple line: Antigen(10ng); Blue line: Antigen (50 ng); Red line: Antigen (100 ng);
Western Blot
Figure 2:Western blot analysis using ATG16L1 mAb against human ATG16L1 (AA: 11-257) recombinant protein. (Expected MW is 55.8 kDa)
Figure 2:Western blot analysis using ATG16L1 mAb against human ATG16L1 (AA: 11-257) recombinant protein. (Expected MW is 55.8 kDa)
Western Blot
Figure 3:Western blot analysis using ATG16L1 mAb against HEK293 (1) and ATG16L1 (AA: 11-257)-hIgGFc transfected HEK293 (2) cell lysate.
Figure 3:Western blot analysis using ATG16L1 mAb against HEK293 (1) and ATG16L1 (AA: 11-257)-hIgGFc transfected HEK293 (2) cell lysate.
Western Blot
Figure 4:Western blot analysis using ATG16L1 mouse mAb against Hela (1), Raji (2), PANC-1 (3), Jurkat (4), PC-12 (5), HepG2 (6), Hek293 (7), and NIH3T3 (8) cell lysate.
Figure 4:Western blot analysis using ATG16L1 mouse mAb against Hela (1), Raji (2), PANC-1 (3), Jurkat (4), PC-12 (5), HepG2 (6), Hek293 (7), and NIH3T3 (8) cell lysate.
Flow cytometric
Figure 5:Flow cytometric analysis of Hela cells using ATG16L1 mouse mAb (green) and negative control (red).
Figure 5:Flow cytometric analysis of Hela cells using ATG16L1 mouse mAb (green) and negative control (red).
For Research Use Only. Not for use in diagnostic procedures.